Amiodarone Hydrochloride Injection recall: Particulate Matter
Amiodarone Hydrochloride Injection, USP, 900 mg per 18 mL (50 mg / mL), 18 mL Multiple Dose Vial, Rx only, Distributed by AuroMedics Pharma LLC E. Windsor, NJ. 08520, Made in India. NDC 55150-182-18
Why was Amiodarone Hydrochloride Injection recalled?
Crystallization: Presence of visible particulate matter.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot#: CAH180013, CAH180014, exp. date Jul 2020
- Product
- Amiodarone Hydrochloride Injection, USP, 900 mg per 18 mL (50 mg / mL), 18 mL Multiple Dose Vial, Rx only, Distributed by AuroMedics Pharma LLC E. Windsor, NJ. 08520, Made in India. NDC 55150-182-18
- Recalling firm
- AuroMedics Pharma LLC
- Quantity
- 138,720 vials
- Distribution
- Distributed Nationwide in the US
- Recall date
- December 4, 2019
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)